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BANP encodes a protein that binds to matrix attachment regions. Zusätzlich bieten wir Ihnen Protein BANP Antikörper (40) und Protein BANP Kits (17) und viele weitere Produktgruppen zu diesem Protein an.
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Dysregulated circ-BANP appears to have an important role in colorectal cancer cells.
results reveal the complex molecular mechanism underlying SMAR1-mediated signal-dependent and -independent regulation of alternative splicing via Sam68 (zeige KHDRBS1 Proteine) deacetylation
SMAR1-mediated regulation of repair and apoptosis via a complex crosstalk involving Ku70 (zeige XRCC6 Proteine), HDAC6 (zeige HDAC6 Proteine) and Bax (zeige BAX Proteine).
Data indicate the role of SMAR1 protein in NF-kappaappa B dependent transcriptional regulation of pro-angiogenic chemokine (zeige CCL1 Proteine) interleukin-8 (IL-8 (zeige IL8 Proteine)).
indicate a crucial role for SMAR1 in restraining breast cancer cell migration and suggest the candidature of this scaffold matrix-associated (zeige SMARCA5 Proteine) region-binding protein as a tumor suppressor.
SMAR1 has a role in repressing c-Fos-mediated HPV18 E6 transcription through alteration of chromatin histone deacetylation
During hemin-induced erythroid differentiation, enhanced expression of SMAR1 negatively correlates with miR (zeige MLXIP Proteine)-320a expression.
TCF-4 (zeige TCF4 Proteine), beta-catenin (zeige CTNNB1 Proteine), and SMAR1 tether at the -143-nucleotide site on the HIV LTR to inhibit HIV promoter activity.
Results indicate that SMAR1 is an important player in p300 (zeige EP300 Proteine)-p53 (zeige TP53 Proteine) regulated DNA damage signalling pathway and can exert its effect on apoptosis in a transcription independent manner.
multiple roles of nuclear matrix associated (zeige SMARCA5 Proteine) protein SMAR1 in regulating various cellular target genes involved in cell growth, apoptosis and tumorigenesis.(REVIEW)
SMAR1 transgenic mice exhibited susceptibility to M. tuberculosis infection in vivo irrespective of genetic background. This susceptibility was attributed to downregulation of Th1 (zeige HAND1 Proteine) response and its hallmark cytokine IFN-gamma (zeige IFNG Proteine)
This study reveals a critical role of SMAR1 in maintaining the proinflammatory immune responses by repressing Th1 (zeige HAND1 Proteine) and Th17 cell function and it gives the novel insight into immune regulatory mechanisms.
we report an essential role of the matrix attachment region (MAR)-binding protein SMAR1 in regulating immune response during allergic airway disease
SMAR1, a known transcription factor and tumor suppressor, is directly involved in maintaining regulatory T cell fate decision
Glucose deprivation can induce p53 (zeige TP53 Proteine) internal ribosome entry sites (IRESs) and also increases cytoplasmic abundance of SMAR1 that in turn binds to p53 (zeige TP53 Proteine) IRESs, indicating the role of SMAR1 in controlling translation of p53 (zeige TP53 Proteine) isoforms.
combined action of Foxp3 (zeige FOXP3 Proteine) and SMAR1 restricts effector cytokine production and enhance the production of IL-10 (zeige IL10 Proteine) by colonic Treg cells that controls acute colitis
SMAR1 and p53 (zeige TP53 Proteine) act synergistically to up-regulate GAD65 (zeige GAD2 Proteine) expression upon Streptozotocin treatment.
A novel mechanism of regulation of oxidative stress by ATM (zeige ATM Proteine) through modulation of SMAR1-AKR1a4 complex, is proposed.
C/EBPbeta (zeige CEBPB Proteine) may regulate preadipocyte proliferation through activation of banp and trim35 (zeige TRIM35 Proteine).
TNFalpha (zeige TNF Proteine) mediated regulation of CD40 (zeige CD40 Proteine) expression occurs by dual phosphorylation of SMAR1 and STAT1 (zeige STAT1 Proteine).
This gene encodes a protein that binds to matrix attachment regions. The protein forms a complex with p53 and negatively regulates p53 transcription, and functions as a tumor suppressor and cell cycle regulator. Multiple transcript variants encoding different isoforms have been found for this gene.
, BTG3 associated nuclear protein
, BEN domain-containing protein 1
, scaffold/matrix-associated region-1-binding protein
, btg3-associated nuclear protein